Danya F Vears

Danya F Vears

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Danya F Vears

Publications by authors named "Danya F Vears"

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Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing.

Eur J Med Genet 2020 Mar 28;63(3):103749. Epub 2019 Aug 28.

Center for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Belgium; Leuven Institute for Human Genetics and Society, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2019.103749DOI Listing
March 2020

On the Epistemic Status of Prenatal Ultrasound: Are Ultrasound Scans Photographic Pictures?

J Med Philos 2020 Mar;45(2):231-250

Centre for Biomedical Ethics and Law, Leuven, Belgium.

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http://dx.doi.org/10.1093/jmp/jhz039DOI Listing
March 2020

Genetic health professionals' experiences with initiating reanalysis of genomic sequence data.

Fam Cancer 2020 Mar 21. Epub 2020 Mar 21.

Center for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1007/s10689-020-00172-7DOI Listing
March 2020

Why genomics researchers are sometimes morally required to hunt for secondary findings.

BMC Med Ethics 2020 01 31;21(1):11. Epub 2020 Jan 31.

Biomedical Ethics Research Group, Murdoch Children's Research Institute, Melbourne, Australia.

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http://dx.doi.org/10.1186/s12910-020-0449-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995186PMC
January 2020

Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients.

J Genet Couns 2019 Dec 19. Epub 2019 Dec 19.

Department of Public Health and Primary Care, Center for Biomedical Ethics and Law, KU Leuven, Belgium.

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http://dx.doi.org/10.1002/jgc4.1209DOI Listing
December 2019

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.

Eur J Hum Genet 2018 12 24;26(12):1743-1751. Epub 2018 Aug 24.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Kapucijnenvoer 35 Box 7001, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1038/s41431-018-0239-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244391PMC
December 2018

Reproductive autonomy in expanded carrier screening: more than meets the eye?

Expert Rev Mol Diagn 2018 12 8;18(12):993-994. Epub 2018 Nov 8.

a Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care , University of Leuven , Leuven , Belgium.

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https://www.tandfonline.com/doi/full/10.1080/14737159.2018.1
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http://dx.doi.org/10.1080/14737159.2018.1544496DOI Listing
December 2018

A systematic analysis of online marketing materials used by providers of expanded carrier screening.

Genet Med 2018 09 14;20(9):976-984. Epub 2017 Dec 14.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/gim.2017.222DOI Listing
September 2018

Key Implications of Data Sharing in Pediatric Genomics.

JAMA Pediatr 2018 05;172(5):476-481

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1001/jamapediatrics.2017.5500DOI Listing
May 2018

Health, wealth and behavioural change: an exploration of role responsibilities in the wake of epigenetics.

J Community Genet 2018 Apr 18;9(2):153-167. Epub 2017 Jul 18.

Freie Universität Berlin, Focus Area DynAge, Berlin, Germany.

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http://dx.doi.org/10.1007/s12687-017-0315-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849698PMC
April 2018

Readability of informed consent forms for whole-exome and whole-genome sequencing.

J Community Genet 2018 Apr 31;9(2):143-151. Epub 2017 Aug 31.

Centre for Research Ethics and Bioethics, Uppsala University, Box564, SE-751 22, Uppsala, Sweden.

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http://dx.doi.org/10.1007/s12687-017-0324-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849699PMC
April 2018

Predictive Psychiatric Genetic Testing in Minors: An Exploration of the Non-Medical Benefits.

J Bioeth Inq 2018 03 11;15(1):111-120. Epub 2017 Dec 11.

Center for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Kapucijnenvoer 35, Box 7001, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s11673-017-9828-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897476PMC
March 2018

Correction to: Predictive Psychiatric Genetic Testing in Minors: An Exploration of the Non-Medical Benefits.

J Bioeth Inq 2018 03;15(1):121

Center for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Kapucijnenvoer 35, Box 7001, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s11673-018-9851-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828493PMC
March 2018

"They Just Want to Know" - Genetic Health Professionals' Beliefs About Why Parents Want to Know their Child's Carrier Status.

J Genet Couns 2017 Dec 4;26(6):1314-1323. Epub 2017 Feb 4.

Centre for Health Equity, Melbourne School of Population and Global Health, University of Melbourne, Parkville, Australia.

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http://dx.doi.org/10.1007/s10897-017-0070-2DOI Listing
December 2017

Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers.

Best Pract Res Clin Obstet Gynaecol 2017 Oct 16;44:57-67. Epub 2017 Feb 16.

Centre for Biomedical Ethics and Law, University of Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bpobgyn.2017.02.006DOI Listing
October 2017

Reporting practices for variants of uncertain significance from next generation sequencing technologies.

Eur J Med Genet 2017 Oct 1;60(10):553-558. Epub 2017 Aug 1.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven - University of Leuven, Leuven, Belgium; Leuven Institute for Human Genomics and Society, KU Leuven - University of Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2017.07.016DOI Listing
October 2017

Reply to C Harling.

Eur J Hum Genet 2017 09 31;25(9):1030. Epub 2017 May 31.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2017.89DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558177PMC
September 2017

Genetic epilepsy with febrile seizures plus: Refining the spectrum.

Neurology 2017 Sep 25;89(12):1210-1219. Epub 2017 Aug 25.

From the Epilepsy Research Centre, Department of Medicine (Y.-H.Z., R.B., J.P.M., G.C.G., K.L.H., L.V., B.E.G., S.T.B., D.F.V., J.A.D., M.S.H., S.F.B., I.E.S.), The University of Melbourne, Austin Health, Australia; Department of Pediatrics (Y.-H.Z.), Peking University First Hospital, Beijing, China; Department of Neurology (L.V.), The University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, Australia; Schneider Children's Medical Center of Israel (S.K., H.G.-S.), Petach Tikvah; Department of Neurology (Z.A.), Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel; Westmead Hospital (A.B.), New South Wales, Australia; Department of Neurology (P.G.-S.), Sydney Children's Hospital, Australia; Department of Neurology (A.D.K.), Tel Aviv University, Israel; Women's and Children's Hospital (L.M.D.), University of Adelaide, South Australia; Center for Neurobehavioral Genetics (E.K.R.), Semel Institute, David Geffen School of Medicine, University of California, Los Angeles; Department of Paediatrics (I.E.S.), The University of Melbourne, Royal Children's Hospital, Victoria; and The Florey Institute of Neurosciences and Mental Health (I.E.S.), Melbourne, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000004384DOI Listing
September 2017

Reporting practices for unsolicited and secondary findings from next-generation sequencing technologies: Perspectives of laboratory personnel.

Hum Mutat 2017 08 6;38(8):905-911. Epub 2017 Jun 6.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/humu.23259DOI Listing
August 2017

Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists' views.

BMC Med Ethics 2017 Aug 1;18(1):46. Epub 2017 Aug 1.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven - University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1186/s12910-017-0206-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539885PMC
August 2017

Ethical sharing of health data in online platforms - which values should be considered?

Life Sci Soc Policy 2017 Aug 21;13(1):12. Epub 2017 Aug 21.

Centre for the Study of Bioethics, University of Belgrade, Belgrade, Serbia.

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http://dx.doi.org/10.1186/s40504-017-0060-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563504PMC
August 2017

Unsolved challenges in pediatric whole-exome sequencing: A literature analysis.

Crit Rev Clin Lab Sci 2017 03 28;54(2):134-142. Epub 2017 Jan 28.

c Department of Public Health and Primary Care , Leuven Institute for Human Genomics and Society , KU Leuven , Leuven , Belgium and.

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http://dx.doi.org/10.1080/10408363.2016.1275516DOI Listing
March 2017

Genomic newborn screening: public health policy considerations and recommendations.

BMC Med Genomics 2017 02 21;10(1). Epub 2017 Feb 21.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1186/s12920-017-0247-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320805PMC
February 2017

Parents' experiences with requesting carrier testing for their unaffected children.

Genet Med 2016 12 24;18(12):1199-1205. Epub 2016 Mar 24.

Centre for Health Equity, Melbourne School of Population and Global Health, University of Melbourne, Parkville, Australia.

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http://dx.doi.org/10.1038/gim.2016.24DOI Listing
December 2016

Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.

J Genet Couns 2016 12 19;25(6):1257-1266. Epub 2016 May 19.

Centre for Health Equity, Melbourne School of Population and Global Health, University of Melbourne, Parkville, Australia.

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http://dx.doi.org/10.1007/s10897-016-9964-7DOI Listing
December 2016

Participation of Children in Medical Decision-Making: Challenges and Potential Solutions.

J Bioeth Inq 2016 Dec 21;13(4):525-534. Epub 2016 Sep 21.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care Faculty of Medicine, Leuven University, Kapucijnenvoer 35, Box 7001, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s11673-016-9747-8DOI Listing
December 2016

Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing.

Eur J Hum Genet 2016 11 15;24(11):1559-1564. Epub 2016 Jun 15.

Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2016.61DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110060PMC
November 2016

Carrier testing in children and adolescents.

Eur J Med Genet 2015 Dec 10;58(12):659-67. Epub 2015 Nov 10.

Genetics Education and Health Research, Murdoch Childrens Research Institute, The Royal Children's Hospital and Department of Paediatrics, The University of Melbourne, Parkville, Australia.

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http://dx.doi.org/10.1016/j.ejmg.2015.11.006DOI Listing
December 2015

Genome-based newborn screening: a conceptual analysis of the best interests of the child standard.

Per Med 2015 Sep 3;12(5):439-441. Epub 2015 Sep 3.

Centre for Biomedical Ethics & Law, Department of Public Health & Primary Care, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.2217/pme.15.28DOI Listing
September 2015

Carrier testing in children: exploration of genetic health professionals' practices in Australia.

Genet Med 2015 May 18;17(5):380-5. Epub 2014 Sep 18.

1] Centre for Health and Society, Melbourne School of Population and Global Health, University of Melbourne, Parkville, Australia [2] Children's Bioethics Centre, Royal Children's Hospital, Parkville, Australia.

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http://dx.doi.org/10.1038/gim.2014.116DOI Listing
May 2015

"It's good to know": experiences of gene identification and result disclosure in familial epilepsies.

Epilepsy Res 2015 May 16;112:64-71. Epub 2015 Feb 16.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Melbourne, Australia; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, Australia; The Florey Neurosciences Institutes (Austin), Melbourne, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2015.02.011DOI Listing
May 2015

Clinical genetic study of the epilepsy-aphasia spectrum.

Epilepsia 2013 Feb 7;54(2):280-7. Epub 2013 Jan 7.

Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1111/epi.12065DOI Listing
February 2013

Efficacy of the ketogenic diet: which epilepsies respond?

Epilepsia 2012 Mar 6;53(3):e55-9. Epub 2012 Feb 6.

Children's Neuroscience Centre, Royal Children's Hospital, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1111/j.1528-1167.2011.03394.xDOI Listing
March 2012

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.

Epilepsia 2012 Feb 5;53(2):319-24. Epub 2012 Jan 5.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1111/j.1528-1167.2011.03368.xDOI Listing
February 2012

Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.

Epilepsia 2011 Oct 21;52(10):e139-42. Epub 2011 Jul 21.

Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, Adelaide, South Australia, Australia.

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http://dx.doi.org/10.1111/j.1528-1167.2011.03188.xDOI Listing
October 2011

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.

Brain 2010 Nov 23;133(11):3221-31. Epub 2010 Sep 23.

Department of Medicine and Epilepsy Research Centre, University of Melbourne, Austin Health, West Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1093/brain/awq251DOI Listing
November 2010

Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTS.

Epilepsia 2009 Oct 9;50(10):2276-84. Epub 2009 Mar 9.

Brain Research Institute, Florey Neuroscience Institutes (Austin), Melbourne, Australia.

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http://dx.doi.org/10.1111/j.1528-1167.2009.02065.xDOI Listing
October 2009